Random homozygous gene perturbation to enhance antibody production

ABSTRACT

The invention reflects enhanced antibody expression of an antibody of interest by cell lines transformed by random homozygous gene perturbation methods to either increase or decrease the expression pattern of a gene of the cell line other than the antibody of interest. The transformed cell line exhibits specific productivity rates, SPR, for the RHGP transformed cell liens of 1.5 or more, as compared with the antibody expressing cell line parents prior to transformation by RHGP. A knock out or anti-sense construct may be devised to reduce expression of the target gene, a promoter may be inserter to enhance expression of the target gene. The antibodies expressed by the transformed cell lines exhibit the binding properties of their parent cell lines prior to transformation with RHGP, and increase Total Volumetric Production of said antibody by said cells in a given volume.

CROSS REFERENCE TO RELATED CASES

This application is a utility application claiming benefit of U.S.provisional application Ser. No. 60/855,127, filed Oct. 30, 2006, whichis incorporated by reference in its entirety herein for all purposes.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made, in part, with U.S. government support underDefense Advanced Research Project Agency (DARPA) Agreement No.W91NF-050C0059. The United States Government may enjoy certain rightspursuant thereto.

BACKGROUND

1. Technical Field

The present invention relates to methods of altering cells to enhanceproduction of proteins they have been raised to express. Particularly,this invention addresses the use of Random Homozygous Gene Perturbationto enhance antibody expression of an antibody-expressing host, bytargeted insertion of DNA to either depress endogenous expression of ahost protein, or enhance expression of a poorly expressed host protein,the change in expression being related to an increase in expression ofthe antibody expressed by the host cell.

2. Background of the Technology

Antibodies, particularly monoclonal antibodies, have become importantbiologic products both in mankind's arsenal against disease, and inresearch and development. While not the “magic bullet” once envisioned,more than a score of monoclonal antibodies, sometimes referred to asmAb, have been approved for therapeutic use. Just a few of these includethe Trastuzumab antibody, the active agent in Herceptin® approved forthe treatment of some breast cancers, Palivizumab, the mAb of Synagis®approved for the prevention/treatment of RSV, and Bevacizumab, a mAbpresent in Avastin®, approved for the treatment of colorectal cancer,and indicated to be effective in treating other conditions. Many moreare known.

By contrast, there are literally thousands of antibodies, mAb andpolyclonal, employed as workhorses in laboratories and researchfacilities around the world. Antibodies are useful as diagnostics, asagents to bind and isolate target molecules, to differentiate cells fortesting, and other uses that take advantage of the specific bindingproperties of IgG to select out a single antigen, typically a biologicalmolecule, bound or unbound, that may be of interest. Antibody productionis fundamental business.

Methods of making antibodies are well established, although refinementsare added constantly. The basic information was set forth as early as1975, Kohler & Milstein, Nature, 256: 495-497 (1975). To preparemonoclonal antibodies, a host, typically a rabbit or the like, isinjected with the antigen against which a mAb is sought. Followingimmunization, the spleen, and possibly lymph nodes, of the host areremoved and separated into single cells. These cells are then exposed tothe target antigen. Cells that express the desired mAb on their surfacewill bind to the immobilized antigen. These cells are cultured andgrown, and fused with myeloma cells or other immortal cells to formhybridoma, which can be cultured to recover the expressed antibody.

Most antibodies, and virtually all therapeutic antibodies, need to bemodified to avoid inducing a rejection reaction in a patient. The DNAencoding the antibody expressed by the hybridoma is isolated, and can bemodified by the insertion or removal of bases, altered glycosylationprofiles, and manipulation of framework regions and complementarydetermining regions, which affect the affinity and avidity with whichthe antibody binds to its target antigen. The resulting antibodies arehumanized or “human” or otherwise modified (chimeric antibodies andveneered antibodies are common in the art). The state of the art as ofabout 1995 is reflected in U.S. Pat. No. 6,054,561, the relevantdisclosure of which is incorporated herein by reference.

Once prepared and isolated, the DNA encoding the antibody may betransferred to a preferred mammalian cell line for expression in“production” or commercial amounts. It has long been recognized thatChinese Hamster Ovary cells (CHO cells) make excellent expressionvehicles for recombinant or non-endogenous DNA. See U.S. Pat. No.4,816,567. There has been developed a series of DHFR deficient CHO cellstrains, which permit the amplification of inserted DNA encodingspecific proteins or DNA sequences, as set forth in U.S. Pat. No.5,981,214. This latter patent describes the use of homologousrecombination to target a specific gene or expression region of acell—in the case in question, to induce expression of a heterologousgene. Other suitable cell lines include 293HEK cells, HeLa cells, COScells, NIH3T3 cells, Jurkat Cells., NSØ cells and HUVEC cells. Othermammalian cell lines suitable for the expression of recombinant proteinshave been identified in the literature, and are equally suitable for usein the invention of this application.

Once stabilized, current methods to increase production of the valuableantibodies tend to focus on increases the total productivity, that is,high volumetric productivity, so that a given amount of cells produces agiven amount of antibodies. These methods tend to focus on improving themethods and environments used to cultivate the cells, to enhance totalantibody production. In general, antibody production of greater thanabout 1 g/L is required for an industrially competitive process.Individual CHO cells are typically expressing in the range of 10-15pg/cell/day.

Homologous recombination has been used in many contexts since about1985. It was originally employed as a “knock-out” tool, allowing thesuppression of an expressed gene, to study the response of the modifiedcell. Subsequent procedures were developed to allow the silencing oftarget genes. The use of anti-sense knock out constructs using a randomhomozygous knock out method (RHKO) is described, e.g., in Li et al, Cell85: 319-329 (196). In U.S. Patent Publication 20060240021 (U.S. patentapplication Ser. No. 10/524,426 filed Aug. 18, 2003) the use of RHKOtechniques is disclosed to identify the genes involved in rapamycinresistance. The entirety of that disclosure is incorporated herein byreference. The ability to insert a construct into one allele, identifythe cells where that allele has been successfully modified by quickthroughput searching, such as for example by FACS (fluorescenceactivated cell sorter) and similar methods makes this a superiortechnique for selective identification and modification of a cell'sgenome. U.S. Pat. No. 6,835,816, incorporated by reference hereindiscloses the use of this technique in conjunction with genes reflectingtumor susceptibility, including TSG101 genes.

Accordingly, it remains a goal of the industry to find a way to increasethe expression of antibodies, particularly recombinantly preparedantibodies, from expression hosts like CHO cells, 293HEK cells, HeLacells, COS cells, NIH3T3 cells, Jurkat Cells, NSØ cells and HUVEC cells.and others, in a stable and reproducible fashion, using availabletechniques to modify the genome of the cell.

SUMMARY

The invention demonstrates that cells that are good expression vehiclesfor recombinant antibodies can be modified to increase the specificproductivity rate (SPR) of antibody producing cells by a factor of 1.5,2 or even 3 fold above the expression range capable of the cell withoutsuch modification. Thus, by selectively altering the expression profileof the cell, using knock out techniques (Random Homozygous GenePerturbation or RHGP) or expression enhancement techniques by insertingexpression promoters rather than anti-sense RNA or other expressionsuppression constructs, antibody production by the cell can be enhanced.Enhancement values of 3-fold or more, SPR, have been achieved bysuppression of the expression of targeted proteins. Enhanced SPR leadsto enhanced volume productivity, permitting commercial collection of mAbon a heretofore desired but not achieved basis.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic illustration of the process of the invention.

FIG. 2 is a schematic illustration of the modification of a cell linegenome by random homozygous gene perturbation according to theinvention.

FIG. 3 is an illustration of the assays that can be used to demonstrateenhanced antibody expression by cells transformed according to theinvention.

FIG. 4 is an illustration of how the repeated use of FACS sorting assayscan enable sequestration of the cells exhibiting the highest SPR for agiven antibody through the invention.

FIG. 5 is a schematic demonstrating the SPR enrichment for cell linestransformed according to the invention using repeated FACS assays.

FIG. 6 is a graph showing the distribution of SPR for cells modified byRHGP as compared with parent expression values.

FIG. 7 is a graph comparing SPR and TPV for cells exhibiting enhancedSPR values following RHGP t reduce Elmo1 expression levels.

FIG. 8 is a graph showing 3-fold enhancement of SPR and TPV using theprocess of the invention.

FIG. 9 is a four part graph demonstrating correlation of SPR with TVP ofcells transformed with RHGP according to the invention.

FIG. 10 is a graph demonstrating the similarity in binding properties ofantibodies expressed by cells transformed by RHGP to exhibit higher SPRvalues with parent cells of the same cell line that did not undergoRHGP.

FIG. 11 is a graph demonstrating long term stability of CHO cell clonesmodified by RHGP to enhance antibody SPR.

FIG. 12 is a graph demonstrating the presence of elevated SPR and TVP byseveral clones of a CHO cell line obtained by RHGP-induceddownregulation of Elmo1 expression.

FIG. 13 reflects the sequence for the Elmo1 gene of humans, mice, ratsand as present in CHO cells transformed by the invention.

FIG. 14 is a vector map of the plasmid used to induce downregulation ofthe Elmo1 gene through RHGP according to the invention.

FIG. 15 is a blotting photomicrograph demonstrating downregulation ofElmo1 in cells exhibiting enhance antibody production followingtransformation by RHGP.

FIG. 16 is a graph demonstrating the increase in SPR of cells modifiedby RHGP as compared with the decrease in expression of Elmo1.

FIG. 17 is a sequence comparison for the ion transporter protein ofhuman, rat, mouse and CHO cell, a target for RHGP pursuant to theinvention.

DETAILED DESCRIPTION

Applicants' invention resides in the discovery that the SpecificProductivity Rate or value of anti-body producing cells can be enhancedby altering the expression profile of the cell's endogenous genomewithout altering the genomic sequence about the antibody itself. Thus,as noted above, it is possible to insert expression enhancers,amplifiable genes, and the like, proximate to, or with, the insertedheterologous DNA that expresses the mAb of interest. These methods havetheir limits. Applicant's invention lies in the discovery that byinserting a construct at a locus other than that which encodes theantibody itself, protein expression profiles may be altered, therebyincreasing he SPR for the antibody. In many cases, this will involveintroducing a knock-out construct . . . and insert encoding, forexample, anti-sense RNA, to down regulate or suppress expression andeven translation of a particular protein. In other situations, it willinvolve inserting an expression construct, or a construct involving anenhancer or promoter or some other activator that enhances expression ofa non-mAb protein, which is implicated in the mAb synthesis pathway, andthus upregulates mAb expression.

This is conveniently affected, in one example, by insertion of ananti-sense knock-out construct that deactivates or inactivates anunrelated protein. Not all knock-out or down regulation will increasemAb expression. There does not appear to be at this time a way to mapthe proteins whose expression profile can be affected in a way topredict whether that alteration will increase SPR of a given cell.Predictably, there are some proteins whose expression cannot besignificantly downregulated without adversely affecting survival of thecell. By the same token, it is quite possible to increase expression ofcertain proteins to the point where they are toxic to the cell.Applicants' invention lies between these two extremes.

In general, there are two ways to improve antibody yield, theoretically.One is to increase total productivity of a given quantity of antibodies.There are limits on the improvements that can be made without affectingthe individual antibody-expressing cells. While one can improveculture/fermentation conditions, improve spacing and the like, realworld limitations on the cost and capability of processing hardware, thecosts and frequency of media replacements, and the like combine to limitthe improvements available by manipulating the environment in which thecells are grown to fractional or incremental improvements.

An alternative approach is to change the expression characteristics ofthe cells themselves. If substantial improvements in cell SPR can bemade, without huge losses in volumetric productivity, and overallincrease in antibody yield is obtained. Applicants have discovered thatin fact SPR can be increased, as much as 300% or better, without aconcomitant loss in productivity of a given volume of cells, giving anoverall increase in antibody expression. Enhanced Antibody Production(EAP) is thus achieved by insertion of a DNA construct at a locusdistant from the locus of the inserted antibody encoding sequence. Thismakes it possible to increase the level of expression withoutendangering the characteristics of the antibody itself or the insertregion, which may be critical to the expression of the heterologousantibody. Quality control is satisfied by ensuring that the mAb productsof cells exhibiting EAP bind with the same relative avidity and affinityto the same target as cells of the parent strain, before enhancement.

The process is generally indicated in FIG. 1, which constitutes a kindof flow chart for the process of the invention. RGHP is used toinactivate one gene per cell in a population of cells, thus creating aRHGP library. The constituent cells of the library are subjected to ahigh throughput assay system for the detection of enhanced IgGproduction. The cells are altered using a Gene Search Vector (GSV) asillustrated in FIG. 2. When integrated into an allele of the targetcell, the inserted construct is expressed—generating, in the embodimentillustrated, an anti-sense RNA which effectively reduces expression ofthe target protein. In alternative embodiments, the GSV may comprise asequence or fragment which boosts expression of the target protein.

The constituent members of the transformed library are then subjected toa high throughput screening process, to identify candidates exhibitingEAP. One assay in particular that lends itself to this process is FACS.This is because transformed ells that express more antibody on theirsurface will secrete or release more antibodies. Thus, a rapid and highthroughput low cost screening process selects out promising candidateswhose mAb expression level are higher due to transformation by the GSV.To confirm that the high producers are in fact expressing the antibodyof interest, the pool selected is subjected to a conventional ELISAassay, ensuring the antibodies secreted by the selected cells do in factbind to the target antigen.

It will be appreciated that many cells will respond to the initialtransformation by giving some gains in mAb SPR. To achieve the goals ofthis invention, that is enhancing SPR by as much as 1.5 fold, all theway up to 3-fold and beyond, only the most responsive transformants willbe selected. FACS screening, as described above, permits rapididentification of EAP cells, in large amounts. This process isillustrated in FIG. 4, where a first selection of, e.g., the top 5% (thepercentage collected will vary with the cell population, and it may beanything from 25% down to 5% —representative values being between thosetwo endpoints, including 10, 15 and 20 percent by way ofexemplification). This “first cut is expanded, and subjected to a secondround of FACS sorting, again selecting a small percentage of theantibody-expressing cells showing the highest SPR. This secondcollection is then subjected to a third round, through single cellplating and culturing conditions—yielding stable populations ofantibody-expressing cells exhibiting EAP and significantly higher SPRsthan the original parent strain prior to manipulation through RHGP.

As shown by actual example discussed, infra, involving decreasedexpression of the Elmo1 gene, in fact, FACS can be used as describedabove, to enhance antibody-production values, and SPRs, of RHGPtransformed cells. The repeated FACS selection “right-shifts” thepopulation of antibodies, with each sorting giving rise to a populationwith a higher SPR—whether measured by mean, median or mode. The actualutility of FACS sorting according to the invention is illustrated inFIG. 5.

Total volume productivity (TVP) screens are faster and easier to do thanselecting out individual improvements in SPR. Thus, the process can beaccelerated by taking a total productivity measure for all the membersof a transformed library. Since total productivity correlates with SPR,by selecting out high productivity lines, likely sources of high mAbexpressing cell lines are the highest volume productivity cell lines.Thus, FIG. 6 reflects an extinction experiment in which volumeproductivity for an entire library of potential transformants ismeasured, following RHGP. Thus, a number of cell lines actually showinferior volume productivity, while the majority show at least somedegree of improvement, when compared with the non-transformed rent line.

The cell lines giving the highest volume productivity values from theexperiment reflected in FIG. 6 (this was done with the Elmo1 experimentset forth below—giving actual experimental values) were measured for SPRas shown in FIG. 7, All but two of the cell lines giving a higher totalproductivity on a 9-day extinction experiment gave SPR values betterthan the parents—and as show, the parents were selected for an alreadyhigh SPR of 16 pg/cell/day. Cell lines expressing >50 pg/cell/day may besecured through this invention. This is illustrated in FIG. 8, where atleast one cell line, 296C2H, prepared by RHGP insertion of the Elmo1anti-sense RNA exhibited both SPR and volume productivity in excess fthis target value. All of the selected cell lines illustrated showmarked improvements in their SPR when compared to the high-producingparent. Thus, given a simple transformation step well away from the citeof the transforming antibody sequences, significant increases inantibody expression are achieved. The correlation between SPR and totalproductivity is also shown in FIG. 9, which shows growth kinetics forthe various cell lines. Depending on the envisaged facility andindustrial or commercial process, growth kinetics may impact the choiceof the “best” modified cell to select, given relatively similar TVP andSPR.

As noted above, it is important to develop a technique that is not onlysimple, susceptible of application on a rapid throughput format, andcapable of giving substantial improvements in the SPR of a givenmAb-producing cell line, it is essential that the transformation takeplace in a site remote from the antibody sequences themselves, so thatantibody properties are not disturbed. As shown in FIG. 10, theantibodies of the RHGP transformed high SPR cells exhibit bindingcharacteristics not distinguishable from those of the parent strain. InFIG. 10, the parent strain is given as the control. These increases arestable over time. See FIG. 11. Equally important is the transformationinduced by RHGP pursuant to the invention results in stable increases inSPR. As shown in FIG. 12, a number of clones from a single experimentinvolving down regulation of the Elmo1 gene exhibited both higher SPRand higher TVP.

EXAMPLE 1 RHGP using Antisense RNA of the Elmo1 Gene

The Elmo1 gene of C. elegans was identified as important in phagocytosisof apoptotic cells, and for cell migration. Gumienny et al, Cell.107(1): 27-41 (2001). This gene was targeted with an anti-senseknock-out RHGP, in an effort to improve higher antibody SPR in cellsexpressing recombinant antibodies. The general strategy described abovewas employed for this experiment.

Identification of Engulfment Cell Motility 1 Protein Gene Involved inEnhanced Antibody Production.

When the individual phenotypes have been selected for cloning, thetarget gene involved in enhanced antibody production was identified bythe strategy shown in FIG. 1. The vector map for the Elmo1 construct isgiven in FIG. 14.

The full-length CHO ELMO1 cDNA was cloned into the expression vectors ofpCDNA3.1 and pLLexp with both orientations, which allow theover-expression of the ELMO1 protein or production of the antisense RNA.Since the anti-ITP antibody is not available, the CHO ITP cDNA was fusedwith myc taq at its 5′ or 3′ end and cloned into pLLexp expressionvector. The fusion partner, myc taq will provide a domain for detectionfor the expressed ITP protein level.

To verify that the phenotypes with higher SPR have the GSV insertion inthe genomes, the genomic DNA was first subjected to PCR amplification ofthe chloramphenicol acetyltransferase (CAT) gene. Indeed, the PCRanalysis has indicated that all the single clones and the pools selectedby FACS have the CAT gene inserted in the genome. To identify the geneinvolved in the phenotype of clone 296-C2H, the genomic DNA was digestedwith restriction enzymes individually, which allow us to rescue thegenomic DNA along with the GSV. The digested genomic DNA wasre-circulated and used to transform E. coli competent cells. A total of16-24 transformed colonies were picked for DNA preparation andsequencing analysis with the LTR primers near the junctions between theGSV vector and the genomic DNA. The regenerated genomic sequence wastaken for Blast Search in GeneBank. A 450-bp domain of CHO genomic DNAsequence shares 87% identities with the sequence on mouse chromosome 13,in which a gene called engulfment and cell motility1 protein (ELMO1) waslocated. Especially, the further sequencing information revealed thatthe corresponding exon 16 domain of CHO cell s shares 95% homology withmouse counterpart. Although the CHO genome sequence database is notavailable in public databases, it's obvious that the GSV has beenintegrated in the intron between the exon 15 and 16 in 296-C2H genomeand interrupted the ELMO1 gene according to the blast searchinformation. The CMV promoter from the GSV seems to transcribe theantisense RNA and knockdown the ELMO1 gene in the phenotype, which haslead to the antibody production enhancement. The ELMO1 gene has beenidentified from many other species, such as mouse, rat and human, whichhas been reported to be involved in the cells motility and required forcell phagocytosis and cells migration. A 3.7-kb full-length ELMO1 cDNAwas isolated from a CHO cDNA library using a 31 nucleotide primerdesigned from exon 16 of CHO ELMO1. The complete coding sequence ofELMO1 from CHO cells is 2181-bp long encoding 727 amino acids protein.The CHO protein shares 99% homology with mouse, rat and human homolog.(FIG. 13). The cDNA was then cloned in pCDNA3.1 and pLLexp expressionvector with both orientations for validation of the gene in naive cellline (FIG. 14)

As discussed above, downregulation of the Elmo1 gene, followinginsertion of the Elmo1 anti-sense “knockout” construct is correlatedwith high SPR in RGHP clones from this experiment. See FIG. 15.Importantly however, while some downregulation was observed, it waspartial. Elmo-1 is still being produced, as would be expected, given thesingle allele insertion. In contrast, the increase in SPR and TVP wasprofound. The two correlated events, induced by a single round of RHGPfollowed by selection as described above, are shown in a single frame inFIG. 16.

EXAMPLE 2 Ion Transporter Protein

To demonstrate the efficacy of this invention, a second target for RHGPwas selected, this time an ion transport protein. What is of fundamentalimportance is that this experiment demonstrates that proteins can bedownregulated (underexpressed as compared with the parent strainexpressing the antibody of interest) or upregulated (overexpressed ascompared with the unmodified parent strain expressing the antibody ofinterest) and nonetheless give EAP. What is fundamentally important isthat the invention provides a method for modifying the expressionpattern of at least one protein of a genome, coupled with a facilemethod for rapid detection and sequestration of cells expressingantibodies at a significantly higher SPR than the parent cell line priorto transformation by RHGP.

Identification of Ion Transporter Protein Gene Homolog Involved inEnhanced Antibody Production.

Using the same strategy, we have successfully identified the insertionsite of the GSV in the genome of another clone 263-C4G. The genomicsequence contig was taken for Blast Search in GeneBank. The genomic DNAsequence of 263-C4G shares significantly high homology with that onmouse chromosome 13, in which the ion transporter protein gene homolog(ITP) was located 15 kb downstream of the GSV insertion site. Mostlikely, the CMV promoter of GSV has over-expressed the ITP homolog andlead to the enhancement of antibody production in the phenotype.

The cDNA of ITP gene was isolated by RT-PCR with mRNA of 263-C4G. The2043-bp cDNA encodes 681 amino acids protein, which shares 96%identities with rat, and 95% with mouse and human homolog (FIG. 17). TheITP homolog belongs to the sugar-type transporter for the movement ofsubstances such as ions, small molecules and micromolecules.

Methods—Preparation of RNA and Genomic DNA.

The total RNA was isolated from CHO cells using TRIZOL Reagent(Invitrogen). Following the manufacturer's protocol, 5-10×10⁶ CHO cellswere used for each preparation. The mRNA was isolated using oligo dTmagnetic beads (Invitrogen). To isolate the genomic DNA, the CHO cells(5-10×10⁶ cells) were collected and washed once with PBS solution. Thecell pellet was resuspended in 10 ml of lysis buffer containing 0.32 MSucrose, 10 mM Tris pH 7.5, 5 mM MgCl₂ and 1% Triton X-100. The celllysate was centrifuged at 1500×g for 15 min. The supernatant was removedand the pellet was resuspended in 0.5 ml of proteinase K buffercontaining 25 mM EDTA, 150 mM NaCl and 40 mM Tris pH 7.5 and transferredto a 1.5-ml tube. Immediately, 10 μl of 10 mg/ml proteinase K stocksolution and 25 μl of 10% SDS were added to the mixture. The solutionwas mixed gently and incubated at 37° C. overnight. The next day, 5 μlof 10 mg/ml of RNAse A was added and incubated at 37° C. for 2-4 hrs.After RNAse A digestion, the DNA mixture was extracted twice withphenol/isoamyl alcohol/chloroform. The DNA was then precipitated withequal volume of isopropanol and centrifuged at 14000 rpm for 15 min. Thepellet was washed with 70% ethanol and dissolved in 200 μl of TE (pH7.5) buffer. The DNA concentration was determined by OD reading at A₂₆₀.

Genomic DNA Cloning.

To identify the genomic DNA sequence surrounding the GSV insertion site,10 μg of each genomic DNA in 250 μl was digested with restrictionenzyme, such as BamHI and HindIII. The digested DNA was then extractedonce with phenol/isoamyl alcohol/chloroform and precipitated with 2.5volumes of ethanol. The DNA was air dried and dissolved in 30 μl of TEbuffer. The digested DNA was then self-ligated with T4 ligase at 16° C.overnight. The next day, the ligated DNA was precipitated with ethanoland dissolved in 20 μl of TE buffer. The ligated DNA was used forelectroporation with ElectroMax DH10B competent cells. Sixteen coloniesfrom each ligated DNA were grown in 1.5 ml culture for DNA preparationand digestion with the restriction enzyme for size analysis. The plasmidDNA was further analyzed by DNA sequencing.

GenBank Blast Search and Genome Mapping.

The DNA sequences were taken for mouse genome homolog search throughNCBI Blast Search program. When the mouse homolog has been identified atthe insertion site, the genes in that locus surrounding the GSV could bescanned and identified. The orientation of the CMV promoter in GSV willdecide either the gene has been knockdown or over-expressed by RHGP. Ifthere was no homology identified, the DNA sequencing will be continueduntil the mouse homolog has been found.

Construction of the CHO cDNA Library.

The cDNA library was constructed with Invitrogen's SuperScript cDNASystem. Following the manufacturer's protocol, the synthesized doublestranded cDNA was ligated into a vector followed by transformation withElectroMax DH10B competent cells. Two million transformants from theelectroporation mixture were used to inoculate 100 ml of the TB brothmedium at 37° C. for overnight. The plasmid DNA of the library wasisolated with a Qiagen kit.

PCR Amplification of ITP cDNA.

Since the exon sequence of CHO ionic transporter protein is notavailable, the target cDNA was amplified by PCR with degenerate primersdesigned from the mouse ITP homolog. A 734-bp cDNA fragment in themiddle of the gene was first amplified with a pair of degenerate primers(L625: 5′AACGTGGTCAGCAARTGGGA3′ and R1339:

5′TTCACYTCRTGGCCCATCAT3′). The amplified cDNA fragment was completelysequenced. The 5′ and 3′ fragments of the gene were subsequentlyamplified with the primers designed from the known sequences of theinternal fragment combined with the 5′ and 3′ primers designed from themouse ITP homolog. After the 5′ and 3′ fragments of the gene wereamplified and sequenced, the full-length ITP cDNA was finally amplifiedby PCR with the primers designed from both ends of the gene (ITP-L1: 5′CCCTGGCCATGGCGATAGAY 3′ and C4G-R3: 5′ GGTCTGTAAACCTGTGTGCA 3′).

While the present invention has been described with reference to thespecific embodiments thereof, it should be understood by those skilledin the art that various changes may be made and equivalents may besubstituted without departing from the true spirit and scope of theinvention. In addition, many modifications may be made to adapt aparticular situation, material, composition of matter, process, processstep or steps, to the objective, spirit and scope of the presentinvention. Of particular note is the fact that the expression pattern ofat least one gene of a genome of a cell line expressing an antibody ofinterest is altered, followed by rapid screening to identify elevatedSPR. Identification of candidates offering EAP, in terms of both SPR andTVP leads to expansion and stabilization of those cell lines usingstandard procedure, as modified for each cell line type, and in light ofthe modification leading to underexpression or overexpresion of thetargeted gene. All such modifications are intended to be within thescope of the claims appended hereto.

1. A method of enhancing the specific productivity ratio of antibodyexpression of a mammalian cell line which expresses an antibody ofinterest, comprising: altering the expression pattern of at least onegene of the genome of said cell line other than said antibody throughrandom homozygous gene perturbation (RHGP) to either increase ordecrease the level of expression of said gene, screening cells of saidcell line transformed by RHGP to identify those transformed cells thatexhibit a higher specific productivity rate(SPR) for antibody ofinterest as compared with members of said cell line not transformed byRHGP, culturing said cells exhibiting a higher SPR to yield a populationof cells expressing said antibody of interest at an enhanced SPR ascompared with said cell line when not enhanced by RHGP.
 2. The method ofclaim 1, wherein said altering of the expression pattern results in saidat least one gone being expressed at a rate lower than the expression ofsaid gene by said cell line without RHGP transformation.
 3. The methodof claim 1, wherein said altering of the expression pattern results insaid at least one gene being expressed at a rate higher than theexpression of said gene by said cell line without RHGP transformation.4. The method of claim 1, wherein said cells transformed by RHGP arescreened by FACS to identify a small fraction of the transformed cellswith the highest SPR for said antibody of interest to produce a screenedcell collection, said screened cell collection is expanded and subjectedto a second FACS screening to identify a small fraction of screened cellcollection with the highest SPR for said antibody of interest to producea second screened cell collection, screening said cells of said secondscreened cell collection by single cell plating to identify a collectionof cells having a higher SPR for said antibody of interest than those ofsaid screened cell collection or said second screened cell collection.5. The method of claim 1, wherein said cells expressing said antibody ofinterest at an enhanced SPR as compared with said cell line when nottransformed by RHGP exhibit an SPR at least 1.5 times that of cells ofsaid cell line when not enhanced by RHGP.
 6. The method of claim 5,wherein said cells expressing said antibody of interest at an enhancedSPR as compared with said cell line when not transformed by RHGP exhibitan SPR at least 3.0 times that of cells of said cell line when notenhanced by RHGP.
 7. The method of claim 1, wherein said cell line is aChinese Hamster Ovary (CHO) cell line, 293HEK cell line, HeLa cell line,COS cells, NIH3T3 cell line, Jurkat cell line, NSØ cell line or HUVECcell line.
 8. The method of claim 7, wherein said cell line is a CHOcell line.